Advertising of Therapeutic Goods in Australia
Under Review - Revised therapeutic goods advertising requirements are still being finalised by the TGA.
For up-to-date information please contact the ASMI Secretariat (02 9922 5111) or the TGA's advertising section (02 6232 8757).
A comprehensive system of controls operates federally across Australia to regulate the advertising of therapeutic goods. This system comprises three integrated levels of regulation - government regulation, co-regulation and self regulation. These complex controls are in place because therapeutic goods are not ordinary items of commerce and it is particularly important that any marketing of them is socially responsible, encourages only appropriate use of products and does not mislead or deceive.
The key components of the advertising controls are:
- advertising codes
- advertising approval requirements
- complaint mechanisms
- self-monitoring activities
Therapeutic goods include medical devices and all medicines, be they over-the-counter medicines or complementary medicines. Only medicines that are unscheduled, schedule 2, or schedule 3 and in Appendix H of the Poisons Standard, may be advertised to consumers. It is illegal to refer to prescription products/substances in advertisements for therapeutic goods directed to consumers.